US6451156B2 - Pressure-sensitive adhesive sheets and method of fixing functional film - Google Patents

Pressure-sensitive adhesive sheets and method of fixing functional film Download PDF

Info

Publication number
US6451156B2
US6451156B2 US09/789,068 US78906801A US6451156B2 US 6451156 B2 US6451156 B2 US 6451156B2 US 78906801 A US78906801 A US 78906801A US 6451156 B2 US6451156 B2 US 6451156B2
Authority
US
United States
Prior art keywords
sensitive adhesive
pressure
weight
functional film
component
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime, expires
Application number
US09/789,068
Other versions
US20010021452A1 (en
Inventor
Hiroaki Kishioka
Masahiro Ohura
Takao Yoshikawa
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nitto Denko Corp
Original Assignee
Nitto Denko Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Nitto Denko Corp filed Critical Nitto Denko Corp
Assigned to NITTO DENKO CORPORATION reassignment NITTO DENKO CORPORATION ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: KISHIOKA, HIROAKI, OHURA, MASAHIRO, YOSHIKAWA, TAKAO
Publication of US20010021452A1 publication Critical patent/US20010021452A1/en
Application granted granted Critical
Publication of US6451156B2 publication Critical patent/US6451156B2/en
Adjusted expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72Polyisocyanates or polyisothiocyanates
    • C08G18/80Masked polyisocyanates
    • C08G18/8061Masked polyisocyanates masked with compounds having only one group containing active hydrogen
    • C08G18/8083Masked polyisocyanates masked with compounds having only one group containing active hydrogen with compounds containing at least one heteroatom other than oxygen or nitrogen
    • C08G18/809Masked polyisocyanates masked with compounds having only one group containing active hydrogen with compounds containing at least one heteroatom other than oxygen or nitrogen containing silicon
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/62Polymers of compounds having carbon-to-carbon double bonds
    • C08G18/6216Polymers of alpha-beta ethylenically unsaturated carboxylic acids or of derivatives thereof
    • C08G18/625Polymers of alpha-beta ethylenically unsaturated carboxylic acids; hydrolyzed polymers of esters of these acids
    • C08G18/6254Polymers of alpha-beta ethylenically unsaturated carboxylic acids and of esters of these acids containing hydroxy groups
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J7/00Adhesives in the form of films or foils
    • C09J7/10Adhesives in the form of films or foils without carriers
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J7/00Adhesives in the form of films or foils
    • C09J7/30Adhesives in the form of films or foils characterised by the adhesive composition
    • C09J7/38Pressure-sensitive adhesives [PSA]
    • C09J7/381Pressure-sensitive adhesives [PSA] based on macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • C09J7/385Acrylic polymers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2170/00Compositions for adhesives
    • C08G2170/40Compositions for pressure-sensitive adhesives
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2301/00Additional features of adhesives in the form of films or foils
    • C09J2301/30Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier
    • C09J2301/302Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier the adhesive being pressure-sensitive, i.e. tacky at temperatures inferior to 30°C
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2433/00Presence of (meth)acrylic polymer
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/28Web or sheet containing structurally defined element or component and having an adhesive outermost layer
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31551Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
    • Y10T428/31609Particulate metal or metal compound-containing
    • Y10T428/31612As silicone, silane or siloxane

Definitions

  • the present invention relates to sheet- or tape-shaped pressure-sensitive adhesive sheets, which are used to fix a functional film to a display device.
  • Pressure-sensitive adhesive sheets have recently been utilized in various fields because of good bonding operation properties.
  • pressure-sensitive adhesive sheets comprising, as a base component, a homopolymer or copolymer of a monomer containing, as a base, an acrylic polymer (i.e. an alkyl (meth)acrylate) are superior in durability performances such as weathering resistance, heat resistance, deterioration resistance and the like. Therefore, they are used particularly preferably in the fields where these durability performances are required.
  • pressure-sensitive adhesive sheets for example, there has been known a use of bonding/fixing functional films such as conductive film, antiglare film and the like to a display device (glass surface thereof).
  • bonding/fixing functional films such as conductive film, antiglare film and the like
  • acrylic pressure-sensitive adhesive sheets comprising an acrylic polymer, as a base component, and a silane coupling agent incorporated into the acrylic polymer, thereby to improve the adhesion to the glass surface.
  • a silane coupling agent incorporated into the acrylic polymer
  • an object of the present invention is to provide pressure-sensitive adhesive sheets for fixing a functional film to a display device, having excellent weathering resistance which cause neither lifting nor formation of bubbles at the bonding interface even when exposed to severe conditions such as high temperature or high temperature and humidity (e.g. inside of automobiles or warehouses in the summer season) for a long time, thus making it possible to maintain good appearance.
  • pressure-sensitive adhesive sheets having excellent weathering resistance wherein the pressure-sensitive adhesive has a crosslinked structure
  • the present invention is directed to a pressure-sensitive adhesive sheet comprising a layer of a crosslinked pressure-sensitive adhesive, which is formed by an acrylic polymermade of a homopolymer or copolymer of a monomer containing a (meth) acrylate as a principal component, a silane coupling agent and a crosslinking agent, wherein a sol component of the crosslinked pressure-sensitive adhesive has a weight-average molecular weight of not less than 300,000 and a proportion of a low-molecular component having a molecular weight of not more than 100,000 in the sol component is not more than 15% by weight in the measurement of the molecular weight by the gel permeation chromatography method. Also the present invention is directed to a method of fixing a functional film, which comprises bonding/fixing the functional film to a display device through the pressure-sensitive adhesive sheets with the constitution described above.
  • the sol component of the layer of the crosslinked pressure-sensitive adhesive refers to a sol component which is a soluble polymer dissolved in ethyl acetate when a predetermined amount Mo (about 0.5 g) of the above layer is covered with a fluororesin film having numerous pores (diameter: 0.2 ⁇ m), followed by dipping in ethyl acetate at 20° C. for 240 hours.
  • the sol fraction thereof is determined by calculating from the formula: (Mt/Mo) ⁇ 100 (% by weight) where Mt is an amount of the sol component and Mo is an initial weight before dipping.
  • the weight-average molecular weight of the sol component and the proportion (% by weight) of the low-molecular component having a molecular weight of not more than 100,000 were determined from a molecular weight distribution curve by the gel permeation chromatography method (hereinafter referred to as the GPC method).
  • the measuring conditions of the molecular weight distribution curve by the GPC method are as follows: concentration of sample; 1 mg/ml, amount of sample introduced; 500 mg, column temperature; 40° C., and flow rate; 1.0 ml/minute.
  • pressure-sensitive adhesive sheets is a general term for pressure-sensitive adhesive tapes and various adhesive products (e.g. pressure-sensitive adhesive labels) having the shape which resembles closely to that of the pressure-sensitive adhesive tapes.
  • the acrylic polymer used as the base polymer in the present invention is a homopolymer or copolymer of a monomer containing an alkyl (meth)acrylate as a principal component, and the other monomer, capable of copolymerizing with the alkyl (meth)acrylate, can be used in combination with the alkyl (meth)acrylate.
  • the alkyl (meth)acrylate is a monomer represented by the following general formula:
  • R 1 is a hydrogen atom or a methyl group
  • R 2 is an alkyl group having 1 to 18 carbon atoms. Specific examples thereof include methyl (meth)acrylate, ethyl (meth)acrylate, propyl (meth)acrylate, butyl (meth)acrylate, 2-ethylhexyl (meth)acrylate, octyl (meth)acrylate, nonyl (meth)acrylate, lauryl (meth)acrylate and the like.
  • the copolymerizable monomer for example, there can be used any of various monomers, which are known as a monomer for modification of an acrylic pressure-sensitive adhesive, such as vinyl acetate, styrene, (meth)acrylonitrile, (meth)acrylamide, (meth)acrylic acid, 2-hydroxyethyl (meth)acrylate, 4-hydroxybutyl (meth)acrylate, 6-hydroxyhexyl (meth)acrylate, glycidyl (meth)acrylate, N,N-dimethylaminoethyl (meth)acrylate and the like.
  • These copolymerizable monomers are usually used in the proportion of not more than 50% by weight based on the total amount of the alkyl (meth)acrylate and the copolymerizable monomer.
  • Such an acrylic polymer is preferably a polymer which exhibits a proper molecular weight distribution before crosslinking, particularly the low-molecular component exhibits a molecular weight smaller than as usual, so that the sol component has a weight-average molecular weight of not less than 300,000, preferably not less than 500,000 (usually up to 5,000,000), and the amount of a low-molecular component having a molecular weight of not more than 100,000 is not more than 15% by weight, preferably not more than 10% by weight by weight in the measurement of the molecular weight by the gel permeation chromatography method after forming a crosslinked structure by the acrylic polymer, the silane coupling agent and the crosslinking agent.
  • the molecular weight constitution of the sol component after crosslinking can be easily set within the above range by using the acrylic polymer with such a constitution to a proper crosslinking treatment.
  • the acrylic polymer with the above constitution can be obtained, for example, by polymerizing due to a solution polymerization method, an emulsion polymerization method or a bulk polymerization method using a polymerization initiator such as azo compound orperoxide, orphotopolymerizing due to irradiation with light using a photopolymerization initiator, or polymerizing due to irradiation with radiation to obtain an acrylic polymer, adding an organic solvent capable of dissolving on a low-molecular component, and removing only the low-molecular component with separating; or adding a required additive to the polymer, forming the mixture into a tape, and treating the tape with the same organic solvent as described above, thereby to elute the low-molecular component.
  • a polymerization initiator such as azo compound orperoxide
  • photopolymerizing due to irradiation with light using a photopolymerization initiator or polymerizing due to irradiation with radiation to obtain an acrylic polymer
  • an acrylic polymer with less low-molecular component can be obtained by using a polymerization solvent having a small chain transfer coefficient in the solution polymerization and polymerizing at the temperature as low as possible due to an increase of the monomer concentration, or employing the photopolymerization method using a photopolymerization initiator, that is, selecting the operation conditions on polymerization.
  • the polymerization operation and the operation of removing the low-molecular component after polymerization may be appropriately used in combination.
  • examples of the silane coupling agent to be incorporated into the acrylic polymer include vinyltrichlorosilane, vinyltris ( ⁇ -methoxyethoxy)silane, vinyltriethoxysilane, vinyltrimethoxysilane, ⁇ -methacryloxypropyltrimethoxysilane, ⁇ -(3,4-epoxycyclohexyl)ethyltrimethoxysilane, ⁇ -glycidoxypropyltrimethoxysilane, ⁇ -glycidoxypropyltriethoxysilane, N- ⁇ (aminoethyl) ⁇ -aminopropyltrimethoxysilane, N- ⁇ (aminoethyl) ⁇ -aminopropylmethyldimethoxysilane, ⁇ -aminopropyltriethoxysilane, N-phenyl- ⁇ -aminopropyltrimethoxysilane, ⁇ -chloropropyl
  • the amount of the silane coupling agent is usually within a range from 0.001 to 5 parts by weight, and preferably from 0.01 to 1 parts by weight, based on 100 parts by weight of the acrylic polymer.
  • the amount of the silane coupling agent is too small, the adhesion to the display device (glass) can not be sufficiently improved.
  • the amount is too large, an adverse influence is likely to be exerted on the bonding properties, which is not preferred.
  • the kind and amount of the crosslinking agent are appropriately selected so that the sol fraction after crosslinking, that is, the proportion of the soluble polymer is usually within a range from 5 to 60% by weight, and preferably from 10 to 40% by weight, and the weight-average molecular weight with respect to the sol component after crosslinking and the proportion of the lower-molecular component having a molecular weight of not more than 100,000, which are determined by the measurement of the molecular weight by the gel permeation chromatography method, are within the above range.
  • the crosslinking agent include conventionally known crosslinking agents, a polyfunctional melamine compound and/or a polyfunctional epoxy compound are particularly preferred. Specific examples thereof include methylatedmethylolmelamine, butylated hexamethylolmelamine, diglycidylaniline, glycerin diglicidyl ether and the like.
  • the amount of the crosslinking agent is usually within a range from 0.001 to 10 parts by weight, and preferably from 0.01 to 5 parts by weight, based on 100 parts by weight of the acrylic polymer.
  • a polyfunctional isocyanate compound is also preferred, and examples of such a compound include tolylene diisocyanate, hexamethylene diisocyanate, polymethylenepolyphenyl isocyanate, diphenylmethane diisocyanate, trimethylolpropanetolylene diisocyanate, polyether polyisocyanate, polyester polyisocyanate and the like.
  • the amount of such a compound is usually within a range from 0.01 to 20 parts by weight, and preferably from 0.05 to 15 parts by weight, based on 100 parts by weight of the acrylic polymer.
  • the pressure-sensitive adhesive sheets of the present invention has a layer of the pressure-sensitive agent crosslinked with the crosslinking agent, which usually has a thickness within a range from 5 to 500 ⁇ m, and preferably from 10 to 100 ⁇ m.
  • This layer may be formed into a sheet or tape by forming on one or both surfaces of a transparent substrate made of a plastic film having a thickness within a range from 10 to 1,000 ⁇ m, or may be formed into the same form described above with no substrate by forming on a proper release liner.
  • These pressure-sensitive adhesive sheets have an adhesive strength to glass of not less than 300 g/20 mm width, and preferably not less than 400 g/20 mm width (usually preferably not more than 2000 g/20 mm width), and are used particularly preferably as an adhesive fixing material for fixing composite films having various functions, which usually have a thickness within a range from about 50 to 200 ⁇ m (for example, functional films such as conductive film, antiglare film, heat ray screening film, anti-reflective sheet, etc.) to a display device (glass surface thereof)
  • the both are bonded/fixed through the pressure-sensitive adhesive sheets.
  • the pressure-sensitive adhesive sheets are applied to the functional film and the resultant is applied to the display device (glass surface thereof).
  • the functional film can be fixed with good adhesive strength without causing lifting and formation of bubbles at the bonding interface when exposed to severe conditions such as high temperature or high temperature and humidity (e.g. inside of automobiles or warehouses in the summer season) for a long time, not to mention at the beginning of standing after bonding, thus making it possible to maintain good appearance for a long term.
  • the reason why such an effect is exerted is not apparent, necessarily.
  • the present inventors consider the reason as follows. That is, an improvement in adhesion to the adherend (display device: glass, etc.) due to incorporation of the silane coupling agent and the constitution of the polymer wherein the amount of the low-molecular component in the sol component after is reduced after crosslinking with the crosslinking agent exerts an action of inhibiting a gas evolved from the pressure-sensitive adhesive sheets, the functional film or the like from causing formation of bubbles and lifting.
  • the acrylic polymer solution A and the acrylic polymer solution B were mixed in a weight ratio of 1:1 to obtain an acrylic polymer solution C having a solid content of 35% by weight.
  • a pressure-sensitive adhesive solution To 100 parts of the acrylic polymer solution B, 1.5 parts of tolylene diisocyanate and 0.09 parts of ⁇ -glycidoxypropyltrimethoxysilane were added to prepare a pressure-sensitive adhesive solution. This solution was spread over a substrate made of a polyethylene terephthalate film having a thickness of 188 ⁇ m so that the thickness after drying becomes 25 ⁇ m, dried with heating at 130° C. for three minutes and then aged at 50° C. for 72 hours to form a pressure-sensitive adhesive sheet for measurement of the adhesive strength, which has a layer of a crosslinked pressure-sensitive adhesive.
  • a pressure-sensitive adhesive sheet for measurement of the weathering resistance comprising a release liner made of a polyethylene terephthalate film having a thickness of 38 ⁇ m and a layer having a thickness of 25 ⁇ m of a crosslinked pressure-sensitive adhesive formed on the release liner was produced.
  • a pressure-sensitive adhesive solution To 100 parts of the acrylic polymer solution C, 3 parts of diphenylmethane diisocyanate and 0.12 parts of ⁇ -methacryloxypropyltrimethoxysilane were added to prepare a pressure-sensitive adhesive solution. In the same manner as in Example 1, a pressure-sensitive adhesive sheet for measurement of the adhesive strength and a pressure-sensitive adhesive sheet for measurement of the weathering resistance were produced.
  • Specimens having a width of 20 mm and a length of 120 mm were made from the pressure-sensitive adhesive sheet for measurement of the adhesive strength. Each of these specimens was laminated on a glass plate by moving rollers (2 kg) back and forth once under the atmosphere at 23° C., and then the peel strength was measured at the same temperature using a Tensilon type peeling tester at a peeling rate of 300 mm/minute.
  • Samples were made by laminating the pressure-sensitive adhesive sheet for measurement of the weathering resistance on a polyethylene terephthalate film having a thickness of 125 ⁇ m and fixing the laminate to glass.
  • the weathering evaluation test was performed by exposing each of the resulting samples to the atmosphere at a temperature of 80 or 60° C. and a humidity of 95% RH for each 500 hours. After the completion of the weathering evaluation test, samples where any of appearance defects such as formation of bubbles and lifting is not visually observed at the bonding interface were rated “ ⁇ ”, whereas, samples where formation of bubbles and lifting are slightly observed were rated “ ⁇ ”.
  • Example 2 Example 1
  • Silane coupling agent contained contained contained none Sol Sol fraction 15 10 15 29 component (% by weight) Weight-average 58 47 49 58 molecular weight ( ⁇ 10,000) Low-molecular 6 12 25 6 component (% by weight)
  • the pressure-sensitive adhesive sheets of Examples 1 and 2 according to the present invention exhibit good adhesive strength according to the molecular weight constitution of the sol component in the layer of the crosslinked pressure-sensitive adhesive, and also exhibit excellent weathering resistance because any of formation of bubbles and lifting does not occur at the bonding interface after the weathering evaluation test.
  • the pressure-sensitive adhesive sheet of Comparative Example 1 wherein the molecular weight constitution of the sol component is not within the scope of the present invention, and the pressure-sensitive adhesive sheet which has a molecular weight constitution of the sol component within the scope of the present invention but contains no silane coupling agent of Comparative Example 2 are inferior in weathering resistance.
  • pressure-sensitive adhesive sheets having excellent weathering resistance wherein a sol component having a specific molecular weight distribution with less low-molecular component, are obtained by incorporating a silane coupling agent into an acrylic polymer and crosslinking the acrylic copolymer.
  • a functional film is bonded/fixed to a display device using the resulting pressure-sensitive adhesive sheets, neither lifting nor formation of bubbles occurs at the bonding interface even during the weathering evaluation test, thus making it possible to maintain good appearance for a long period.

Abstract

A pressure-sensitive adhesive sheets comprising a layer of a crosslinked pressure-sensitive adhesive, which is formed by an acrylic polymer made of a homopolymer or copolymer of a monomer containing a (meth)acrylate as a principal component, a silane coupling agent and a crosslinking agent, wherein a sol component of the crosslinked pressure-sensitive adhesive has a weight-average molecular weight of not less than 300,000 and a proportion of a low-molecular component having a molecular weight of not more than 100,000 in the sol component is not more than 15% by weight in the measurement of the molecular weight by the gel permeation chromatography method, which the sheet cause neither lifting nor formation of bubbles at the bonding interface even when exposed to severe conditions such as high temperature or high temperature and humidity in case a functional film is bonded/fixed to a display device, thus making it possible to maintain good appearance for a long period.

Description

BACKGROUND OF THE INVENTION
1. Field of the Invention
The present invention relates to sheet- or tape-shaped pressure-sensitive adhesive sheets, which are used to fix a functional film to a display device.
2. Description of the Related Art
Pressure-sensitive adhesive sheets have recently been utilized in various fields because of good bonding operation properties. Among these, pressure-sensitive adhesive sheets comprising, as a base component, a homopolymer or copolymer of a monomer containing, as a base, an acrylic polymer (i.e. an alkyl (meth)acrylate) are superior in durability performances such as weathering resistance, heat resistance, deterioration resistance and the like. Therefore, they are used particularly preferably in the fields where these durability performances are required.
As one of uses of pressure-sensitive adhesive sheets, for example, there has been known a use of bonding/fixing functional films such as conductive film, antiglare film and the like to a display device (glass surface thereof). In view of use such as display device to which severe requirements on the appearance is made, it is required for these pressure-sensitive adhesive sheets to cause neither lifting nor formation of bubbles at the bonding interface when exposed to severe conditions such as high temperature or high temperature and humidity (e.g. inside of automobiles or warehouses in the summer season) for a long time, not to mention at the beginning of standing after bonding/fixing, thus making it possible to maintain good appearance.
To resolve these requirements, it is suggested to use acrylic pressure-sensitive adhesive sheets comprising an acrylic polymer, as a base component, and a silane coupling agent incorporated into the acrylic polymer, thereby to improve the adhesion to the glass surface. Although use of the pressure-sensitive adhesive sheets improves the adhesion to glass to some extent, there still remains such a problem that lifting and formation of bubbles occur at the bonding interface when exposed to severe conditions such as high temperature or high temperature and humidity (e.g. inside of automobiles or warehouses in the summer season) for a long time, thus making it hard to maintain good appearance.
SUMMARY OF THE INVENTION
In light of the circumstances described above, an object of the present invention is to provide pressure-sensitive adhesive sheets for fixing a functional film to a display device, having excellent weathering resistance which cause neither lifting nor formation of bubbles at the bonding interface even when exposed to severe conditions such as high temperature or high temperature and humidity (e.g. inside of automobiles or warehouses in the summer season) for a long time, thus making it possible to maintain good appearance.
As a result of an intensively study about the object described above, the present inventors have found that pressure-sensitive adhesive sheets having excellent weathering resistance, wherein the pressure-sensitive adhesive has a crosslinked structure, are obtained by incorporating a silane coupling agent into an acrylic polymer and crosslinking the acrylic copolymer, and a sol component of the crosslinked pressure-sensitive adhesive having a specific molecular weight distribution with less low-molecular component, and that, when a functional film is bonded/fixed to a display device using the resulting pressure-sensitive adhesive sheets, neither lifting nor formation of bubbles occurs at the bonding interface even during the weathering evaluation test, thus making it possible to maintain good appearance for a long period, whereby the present invention has been completed.
That is, the present invention is directed to a pressure-sensitive adhesive sheet comprising a layer of a crosslinked pressure-sensitive adhesive, which is formed by an acrylic polymermade of a homopolymer or copolymer of a monomer containing a (meth) acrylate as a principal component, a silane coupling agent and a crosslinking agent, wherein a sol component of the crosslinked pressure-sensitive adhesive has a weight-average molecular weight of not less than 300,000 and a proportion of a low-molecular component having a molecular weight of not more than 100,000 in the sol component is not more than 15% by weight in the measurement of the molecular weight by the gel permeation chromatography method. Also the present invention is directed to a method of fixing a functional film, which comprises bonding/fixing the functional film to a display device through the pressure-sensitive adhesive sheets with the constitution described above.
As used herein, the sol component of the layer of the crosslinked pressure-sensitive adhesive refers to a sol component which is a soluble polymer dissolved in ethyl acetate when a predetermined amount Mo (about 0.5 g) of the above layer is covered with a fluororesin film having numerous pores (diameter: 0.2 μm), followed by dipping in ethyl acetate at 20° C. for 240 hours. The sol fraction thereof is determined by calculating from the formula: (Mt/Mo)×100 (% by weight) where Mt is an amount of the sol component and Mo is an initial weight before dipping.
Using the above soluble polymer (sol component), the weight-average molecular weight of the sol component and the proportion (% by weight) of the low-molecular component having a molecular weight of not more than 100,000 were determined from a molecular weight distribution curve by the gel permeation chromatography method (hereinafter referred to as the GPC method). The measuring conditions of the molecular weight distribution curve by the GPC method are as follows: concentration of sample; 1 mg/ml, amount of sample introduced; 500 mg, column temperature; 40° C., and flow rate; 1.0 ml/minute.
As used herein, the term “pressure-sensitive adhesive sheets” is a general term for pressure-sensitive adhesive tapes and various adhesive products (e.g. pressure-sensitive adhesive labels) having the shape which resembles closely to that of the pressure-sensitive adhesive tapes.
DETAILED DESCRIPTION OF THE INVENTION
The acrylic polymer used as the base polymer in the present invention is a homopolymer or copolymer of a monomer containing an alkyl (meth)acrylate as a principal component, and the other monomer, capable of copolymerizing with the alkyl (meth)acrylate, can be used in combination with the alkyl (meth)acrylate.
The alkyl (meth)acrylate is a monomer represented by the following general formula:
Figure US06451156-20020917-C00001
wherein R1 is a hydrogen atom or a methyl group, and R2 is an alkyl group having 1 to 18 carbon atoms. Specific examples thereof include methyl (meth)acrylate, ethyl (meth)acrylate, propyl (meth)acrylate, butyl (meth)acrylate, 2-ethylhexyl (meth)acrylate, octyl (meth)acrylate, nonyl (meth)acrylate, lauryl (meth)acrylate and the like.
The copolymerizable monomer, for example, there can be used any of various monomers, which are known as a monomer for modification of an acrylic pressure-sensitive adhesive, such as vinyl acetate, styrene, (meth)acrylonitrile, (meth)acrylamide, (meth)acrylic acid, 2-hydroxyethyl (meth)acrylate, 4-hydroxybutyl (meth)acrylate, 6-hydroxyhexyl (meth)acrylate, glycidyl (meth)acrylate, N,N-dimethylaminoethyl (meth)acrylate and the like. These copolymerizable monomers are usually used in the proportion of not more than 50% by weight based on the total amount of the alkyl (meth)acrylate and the copolymerizable monomer.
Such an acrylic polymer is preferably a polymer which exhibits a proper molecular weight distribution before crosslinking, particularly the low-molecular component exhibits a molecular weight smaller than as usual, so that the sol component has a weight-average molecular weight of not less than 300,000, preferably not less than 500,000 (usually up to 5,000,000), and the amount of a low-molecular component having a molecular weight of not more than 100,000 is not more than 15% by weight, preferably not more than 10% by weight by weight in the measurement of the molecular weight by the gel permeation chromatography method after forming a crosslinked structure by the acrylic polymer, the silane coupling agent and the crosslinking agent. The molecular weight constitution of the sol component after crosslinking can be easily set within the above range by using the acrylic polymer with such a constitution to a proper crosslinking treatment.
Before crosslinking, the acrylic polymer with the above constitution can be obtained, for example, by polymerizing due to a solution polymerization method, an emulsion polymerization method or a bulk polymerization method using a polymerization initiator such as azo compound orperoxide, orphotopolymerizing due to irradiation with light using a photopolymerization initiator, or polymerizing due to irradiation with radiation to obtain an acrylic polymer, adding an organic solvent capable of dissolving on a low-molecular component, and removing only the low-molecular component with separating; or adding a required additive to the polymer, forming the mixture into a tape, and treating the tape with the same organic solvent as described above, thereby to elute the low-molecular component.
According to alternative method of forming the acrylic polymer with the above constitution, an acrylic polymer with less low-molecular component can be obtained by using a polymerization solvent having a small chain transfer coefficient in the solution polymerization and polymerizing at the temperature as low as possible due to an increase of the monomer concentration, or employing the photopolymerization method using a photopolymerization initiator, that is, selecting the operation conditions on polymerization. The polymerization operation and the operation of removing the low-molecular component after polymerization may be appropriately used in combination.
In the present invention, examples of the silane coupling agent to be incorporated into the acrylic polymer include vinyltrichlorosilane, vinyltris (β-methoxyethoxy)silane, vinyltriethoxysilane, vinyltrimethoxysilane, γ-methacryloxypropyltrimethoxysilane, β-(3,4-epoxycyclohexyl)ethyltrimethoxysilane, γ-glycidoxypropyltrimethoxysilane, γ-glycidoxypropyltriethoxysilane, N-β(aminoethyl)γ-aminopropyltrimethoxysilane, N-β(aminoethyl)γ-aminopropylmethyldimethoxysilane, γ-aminopropyltriethoxysilane, N-phenyl-γ-aminopropyltrimethoxysilane, γ-chloropropyltrimethoxysilane and the like.
The amount of the silane coupling agent is usually within a range from 0.001 to 5 parts by weight, and preferably from 0.01 to 1 parts by weight, based on 100 parts by weight of the acrylic polymer. When the amount of the silane coupling agent is too small, the adhesion to the display device (glass) can not be sufficiently improved. On the other hand, when the amount is too large, an adverse influence is likely to be exerted on the bonding properties, which is not preferred.
In the present invention, in case the silane coupling agent is incorporated into the acrylic polymer and the acrylic polymer is crosslinked with the crosslinking agent, the kind and amount of the crosslinking agent are appropriately selected so that the sol fraction after crosslinking, that is, the proportion of the soluble polymer is usually within a range from 5 to 60% by weight, and preferably from 10 to 40% by weight, and the weight-average molecular weight with respect to the sol component after crosslinking and the proportion of the lower-molecular component having a molecular weight of not more than 100,000, which are determined by the measurement of the molecular weight by the gel permeation chromatography method, are within the above range.
The crosslinking agent include conventionally known crosslinking agents, a polyfunctional melamine compound and/or a polyfunctional epoxy compound are particularly preferred. Specific examples thereof include methylatedmethylolmelamine, butylated hexamethylolmelamine, diglycidylaniline, glycerin diglicidyl ether and the like. The amount of the crosslinking agent is usually within a range from 0.001 to 10 parts by weight, and preferably from 0.01 to 5 parts by weight, based on 100 parts by weight of the acrylic polymer.
Use of a polyfunctional isocyanate compound is also preferred, and examples of such a compound include tolylene diisocyanate, hexamethylene diisocyanate, polymethylenepolyphenyl isocyanate, diphenylmethane diisocyanate, trimethylolpropanetolylene diisocyanate, polyether polyisocyanate, polyester polyisocyanate and the like. The amount of such a compound is usually within a range from 0.01 to 20 parts by weight, and preferably from 0.05 to 15 parts by weight, based on 100 parts by weight of the acrylic polymer.
The pressure-sensitive adhesive sheets of the present invention has a layer of the pressure-sensitive agent crosslinked with the crosslinking agent, which usually has a thickness within a range from 5 to 500 μm, and preferably from 10 to 100 μm. This layer may be formed into a sheet or tape by forming on one or both surfaces of a transparent substrate made of a plastic film having a thickness within a range from 10 to 1,000 μm, or may be formed into the same form described above with no substrate by forming on a proper release liner.
These pressure-sensitive adhesive sheets have an adhesive strength to glass of not less than 300 g/20 mm width, and preferably not less than 400 g/20 mm width (usually preferably not more than 2000 g/20 mm width), and are used particularly preferably as an adhesive fixing material for fixing composite films having various functions, which usually have a thickness within a range from about 50 to 200 μm (for example, functional films such as conductive film, antiglare film, heat ray screening film, anti-reflective sheet, etc.) to a display device (glass surface thereof)
In the present invention, in order to fix the above functional film to the display device, the both are bonded/fixed through the pressure-sensitive adhesive sheets. Usually, the pressure-sensitive adhesive sheets are applied to the functional film and the resultant is applied to the display device (glass surface thereof). Whereby, the functional film can be fixed with good adhesive strength without causing lifting and formation of bubbles at the bonding interface when exposed to severe conditions such as high temperature or high temperature and humidity (e.g. inside of automobiles or warehouses in the summer season) for a long time, not to mention at the beginning of standing after bonding, thus making it possible to maintain good appearance for a long term.
The reason why such an effect is exerted is not apparent, necessarily. The present inventors consider the reason as follows. That is, an improvement in adhesion to the adherend (display device: glass, etc.) due to incorporation of the silane coupling agent and the constitution of the polymer wherein the amount of the low-molecular component in the sol component after is reduced after crosslinking with the crosslinking agent exerts an action of inhibiting a gas evolved from the pressure-sensitive adhesive sheets, the functional film or the like from causing formation of bubbles and lifting.
EXAMPLES
The present invention will be described in more detail by way of the following Examples. In the Examples, parts are by weight unless otherwise stated. Acrylic polymer solutions A to C used in the following Examples and Comparative Examples are prepared by the following manners.
<Acrylic Polymer Solution A>
70 Parts of 2-ethylhexyl acrylate, 25 parts of n-butyl acrylate, 5 parts of acrylic acid, 0.06 parts of 3-hydroxypropyl acrylate, and 45 parts of ethyl acetate as a polymerization solvent were charged in a three-necked flask, followed by stirring while introducing a nitrogen gas for two hours. After removing oxygen in the polymerization system, 0.2 parts of benzoyl peroxide was added and the mixture was reactedby heating to 60° C. for ten hours, then reacted by heating to 75° C. for two hours. To the reaction solution, ethyl acetate was added to obtain an acrylic polymer solution A having a solid content of 45% by weight.
<Acrylic Polymer Solution B>
To 100 parts of the acrylic polymer solution A, 120 parts of n-heptane was added dropwise while stirring over six hours. After left to stand for 24 hours, the supernatant was separated. To the polymer solution after separating the supernatant, toluene was added and dissolved and, furthermore, the operation of adding 120 parts of n-heptane and separating the supernatant in the same manner as described above was repeated five times. To the final polymer solution thus obtained, 80 parts of toluene was added, followed by concentration to obtain an acrylic polymer solution B having a solid content of 25% by weight.
<Acrylic Polymer Solution C>
The acrylic polymer solution A and the acrylic polymer solution B were mixed in a weight ratio of 1:1 to obtain an acrylic polymer solution C having a solid content of 35% by weight.
Example 1
To 100 parts of the acrylic polymer solution B, 1.5 parts of tolylene diisocyanate and 0.09 parts of γ-glycidoxypropyltrimethoxysilane were added to prepare a pressure-sensitive adhesive solution. This solution was spread over a substrate made of a polyethylene terephthalate film having a thickness of 188 μm so that the thickness after drying becomes 25 μm, dried with heating at 130° C. for three minutes and then aged at 50° C. for 72 hours to form a pressure-sensitive adhesive sheet for measurement of the adhesive strength, which has a layer of a crosslinked pressure-sensitive adhesive. In the same manner as described above, a pressure-sensitive adhesive sheet for measurement of the weathering resistance, comprising a release liner made of a polyethylene terephthalate film having a thickness of 38 μm and a layer having a thickness of 25 μm of a crosslinked pressure-sensitive adhesive formed on the release liner was produced.
Example 2
To 100 parts of the acrylic polymer solution C, 3 parts of diphenylmethane diisocyanate and 0.12 parts of γ-methacryloxypropyltrimethoxysilane were added to prepare a pressure-sensitive adhesive solution. In the same manner as in Example 1, a pressure-sensitive adhesive sheet for measurement of the adhesive strength and a pressure-sensitive adhesive sheet for measurement of the weathering resistance were produced.
Comparative Example 1
To 100 parts of the acrylic polymer solution C, 0.8 parts of trimethylolpropanetolylene diisocyanate and 0.15 parts of β-(3,4-epoxycyclohexyl)trimethoxysilane were added to prepare a pressure-sensitive adhesive solution. In the same manner as in Example 1, a pressure-sensitive adhesive sheet for measurement of the adhesive strength and a pressure-sensitive adhesive sheet for measurement of the weathering resistance were produced using the resulting pressure-sensitive adhesive solution.
Comparative Example 2
To 100 parts of the acrylic polymer solution B, 3 parts of trimethylolpropanetolylene diisocyanate was added to prepare a pressure-sensitive adhesive solution. In the same manner as in Example 1, a pressure-sensitive adhesive sheet for measurement of the adhesive strength and a pressure-sensitive adhesive sheet for measurement of the weathering resistance were produced using the resulting pressure-sensitive adhesive solution.
With respect to the pressure-sensitive adhesive sheets for measurement of the adhesive strength and pressure-sensitive adhesive sheets for measurement of the weathering resistance of Examples 1 and 2 and Comparative Examples 1 and 2, the adhesive strength test and weathering evaluation test were performed in the following procedures. These results are as shown in Table 1. In Table 1, the presence or absence of the silane coupling agent in the pressure-sensitive adhesive solution as well as the sol fraction, the weight-average molecular weight as measured by the GPC method and the proportion of the low-molecular component having the molecular weight of not more than 100,000 with respect to the sol component of the layer of the crosslinked pressure-sensitive adhesive are also shown for reference.
<Adhesive Strength Test>
Specimens having a width of 20 mm and a length of 120 mm were made from the pressure-sensitive adhesive sheet for measurement of the adhesive strength. Each of these specimens was laminated on a glass plate by moving rollers (2 kg) back and forth once under the atmosphere at 23° C., and then the peel strength was measured at the same temperature using a Tensilon type peeling tester at a peeling rate of 300 mm/minute.
<Weathering Evaluation Test>
Samples were made by laminating the pressure-sensitive adhesive sheet for measurement of the weathering resistance on a polyethylene terephthalate film having a thickness of 125 μm and fixing the laminate to glass. The weathering evaluation test was performed by exposing each of the resulting samples to the atmosphere at a temperature of 80 or 60° C. and a humidity of 95% RH for each 500 hours. After the completion of the weathering evaluation test, samples where any of appearance defects such as formation of bubbles and lifting is not visually observed at the bonding interface were rated “◯”, whereas, samples where formation of bubbles and lifting are slightly observed were rated “×”.
TABLE 1
Comparative Comparative
Example 1 Example 2 Example 1 Example 2
Silane coupling agent contained contained contained none
Sol Sol fraction 15 10 15 29
component (% by weight)
Weight-average 58 47 49 58
molecular weight
(×10,000)
Low-molecular 6 12 25 6
component
(% by weight)
Adhesive strength test 550 590 620 500
(g/20 mm width)
Weathering evaluation test X X
As is apparent from Table 1, the pressure-sensitive adhesive sheets of Examples 1 and 2 according to the present invention exhibit good adhesive strength according to the molecular weight constitution of the sol component in the layer of the crosslinked pressure-sensitive adhesive, and also exhibit excellent weathering resistance because any of formation of bubbles and lifting does not occur at the bonding interface after the weathering evaluation test. On the other hand, the pressure-sensitive adhesive sheet of Comparative Example 1 wherein the molecular weight constitution of the sol component is not within the scope of the present invention, and the pressure-sensitive adhesive sheet which has a molecular weight constitution of the sol component within the scope of the present invention but contains no silane coupling agent of Comparative Example 2 are inferior in weathering resistance.
As described above, pressure-sensitive adhesive sheets having excellent weathering resistance, wherein a sol component having a specific molecular weight distribution with less low-molecular component, are obtained by incorporating a silane coupling agent into an acrylic polymer and crosslinking the acrylic copolymer. When a functional film is bonded/fixed to a display device using the resulting pressure-sensitive adhesive sheets, neither lifting nor formation of bubbles occurs at the bonding interface even during the weathering evaluation test, thus making it possible to maintain good appearance for a long period.

Claims (11)

What is claimed is:
1. A pressure-sensitive adhesive sheet comprising a layer of a crosslinked pressure-sensitive adhesive, which is formed by an acrylic polymer made of a homopolymer or copolymer of a monomer containing a (meth)acrylate as a principal component, a silane coupling agent and a crosslinking agent, wherein a sol component of the crosslinked pressure-sensitive adhesive has a weight-average molecular weight of not less than 300,000 and a proportion of a low-molecular component having a molecular weight of not more than 100,000 in the sol component is not more than 15% by weight in the measurement of the molecular weight by the gel permeation chromatography method.
2. The pressure-sensitive adhesive sheet according to claim 1, wherein the amount of the silane coupling agent is within a range from 0.001 to 5 parts by weight based on 100 parts by weight of the acrylic polymer.
3. The pressure-sensitive adhesive sheet according to claim 1, wherein a sol fraction of the sol component of the layer of the crosslinked pressure-sensitive adhesive agent is within a range from 5 to 60% by weight.
4. The pressure-sensitive adhesive sheet according to claim 1, wherein the adhesive strength to glass is not less than 300 g/20 mm width.
5. A method of fixing a functional film, which comprises bonding/fixing the functional film to a display device through the pressure-sensitive adhesive sheets of claim 1.
6. The pressure-sensitive adhesive sheet according to claim 2, wherein a sol fraction of the sol component of the layer of the crosslinked pressure-sensitive adhesive agent is within a range from 5 to 60% by weight.
7. The pressure-sensitive adhesive sheet according to claim 2, wherein the adhesive strength to glass is not less than 300 g/20 mm width.
8. The pressure-sensitive adhesive sheet according to claim 3, wherein the adhesive strength to glass is not less than 300 g/20 mm width.
9. A method of fixing a functional film, which comprises bonding/fixing the functional film to a display device through the pressure-sensitive adhesive sheets of claim 2.
10. A method of fixing a functional film, which comprises bonding/fixing the functional film to a display device through the pressure-sensitive adhesive sheets of claim 3.
11. A method of fixing a functional film, which comprises bonding/fixing the functional film to a display device through the pressure-sensitive adhesive sheets of claim 4.
US09/789,068 2000-02-24 2001-02-20 Pressure-sensitive adhesive sheets and method of fixing functional film Expired - Lifetime US6451156B2 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP2000052243A JP3819661B2 (en) 2000-02-24 2000-02-24 Fixing method of pressure-sensitive adhesive sheets and functional films
JP2000-52243 2000-02-24
JP2000-052243 2000-02-24

Publications (2)

Publication Number Publication Date
US20010021452A1 US20010021452A1 (en) 2001-09-13
US6451156B2 true US6451156B2 (en) 2002-09-17

Family

ID=18573797

Family Applications (1)

Application Number Title Priority Date Filing Date
US09/789,068 Expired - Lifetime US6451156B2 (en) 2000-02-24 2001-02-20 Pressure-sensitive adhesive sheets and method of fixing functional film

Country Status (4)

Country Link
US (1) US6451156B2 (en)
JP (1) JP3819661B2 (en)
KR (1) KR100723113B1 (en)
TW (1) TWI241331B (en)

Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6599967B2 (en) 2000-08-01 2003-07-29 Nitto Denko Corporation Pressure-sensitive adhesive sheet and method of fixing functional film
US20050014879A1 (en) * 2003-02-10 2005-01-20 Yutaka Moroishi Pressure sensitive adhesive composition for optical members, pressure sensitive adhesive layer for optical members, pressure sensitive adhesive optical member and image display
US20080281047A1 (en) * 2007-05-08 2008-11-13 Nitto Denko Corporation Pressure-sensitive adhesive composition, and pressure-sensitive adhesive product and display using the same
US20090023869A1 (en) * 2005-01-25 2009-01-22 Nitto Denko Corporation Pressure sensitive adhesive composition for optical members, pressure sensitive adhesive layer for optical members, pressure sensitive adhesive optical member and image display
US20090022988A1 (en) * 2004-12-02 2009-01-22 Yuusuke Toyama Pressure sensitive adhesives for optical film, manufacturing methods for pressure sensitive adhesive layer for optical film, pressure sensitive adhesive layers for optical film, pressure sensitive adhesion type optical films and image displays
US20090104450A1 (en) * 2007-10-22 2009-04-23 Nitto Denko Corporation Pressure-sensitive adhesive composition for optical film, pressure-sensitive adhesive layer for optical film, production method thereof, pressure-sensitive adhesive optical film and image display
US20090162577A1 (en) * 2007-12-20 2009-06-25 Nitto Denko Corporation Pressure-sensitive adhesive composition for optical films, pressure-sensitive adhesive optical film and image display
CN1683464B (en) * 2004-04-15 2010-05-05 日东电工株式会社 Adhesive composition for optical member, adhesive layer for optical member and its producing method, optical member with adhesive, and image display device
US20100255253A1 (en) * 2009-04-01 2010-10-07 Nitto Denko Corporation Double-sided pressure-sensitive adhesive sheet, production method of double-sided pressure-sensitive adhesive sheet, pressure-sensitive adhesion type optical functional film and pressure-sensitive adhesion type hard coat film
US20100304134A1 (en) * 2008-01-25 2010-12-02 NITTO DENKO CORPORATION a corporation Method for peeling pressure-sensitive adhesive optical film, and pressure-sensitive adhesive optical film
US20110014410A1 (en) * 2009-07-16 2011-01-20 Nitto Denko Corporation Double-sided pressure-sensitive adhesive tape
US20110135810A1 (en) * 2009-12-03 2011-06-09 Marina Yakovleva Finely deposited lithium metal powder
US20120189835A1 (en) * 2011-01-25 2012-07-26 Nitto Denko Corporation Optical pressure-sensitive adhesive sheet
US20130123450A1 (en) * 2011-11-10 2013-05-16 Nitto Denko Corporation Pressure-sensitive adhesive sheet
US20150293287A1 (en) * 2012-08-31 2015-10-15 Nitto Denko Corporation Pressure-sensitive adhesive layer attached polarizing film and image display

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6927267B1 (en) 2002-03-07 2005-08-09 Basf Ag High solids dispersion for wide temperature, pressure sensitive adhesive applications
DE10229733A1 (en) * 2002-07-02 2004-01-22 Basf Ag Pressure sensitive adhesives for carriers made of soft PVC
DE10323048A1 (en) * 2003-05-20 2004-12-09 Basf Ag Pressure sensitive adhesives containing polyethylene
TW200632002A (en) * 2004-11-30 2006-09-16 Fuji Photo Film Co Ltd Polarizing plate and liquid crystal display device comprising the same
US7625596B2 (en) * 2004-12-15 2009-12-01 General Electric Company Adhesion promoter, electroactive layer and electroactive device comprising same, and method
JP4799937B2 (en) * 2005-07-11 2011-10-26 日東電工株式会社 Water-dispersed pressure-sensitive adhesive composition and pressure-sensitive adhesive sheet
JP5268234B2 (en) * 2006-04-25 2013-08-21 日東電工株式会社 Liquid crystal panel and liquid crystal display device
JP5351420B2 (en) * 2008-01-23 2013-11-27 リンテック株式会社 Adhesive sheet and liquid crystal display device
JP2011096988A (en) * 2009-11-02 2011-05-12 Keiwa Inc Adhesive sheet for protecting back of solar cell module, and solar cell module using the same
JP6117478B2 (en) * 2011-04-22 2017-04-19 日東電工株式会社 Adhesive functional film and display device
TWI521032B (en) 2012-06-28 2016-02-11 羅門哈斯公司 Wet glue
KR101622071B1 (en) * 2014-11-01 2016-05-19 삼성에스디아이 주식회사 Adhesive composition, adhesive film prepared by the same and display member comprising the same
DE102015224734A1 (en) * 2015-12-09 2017-06-14 Tesa Se Composition for the production of pressure-sensitive adhesives
CN105644091A (en) * 2015-12-29 2016-06-08 秦皇岛市地维建材有限公司 Preparation method of TPO crossed compound sheet self-adhesion waterproof coiled material
KR102257813B1 (en) 2018-11-13 2021-05-28 주식회사 엘지화학 Adhesive composition and adhesive film prepared therefrom
JP7385053B2 (en) 2021-08-05 2023-11-21 積水化学工業株式会社 Adhesive tape

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01178567A (en) 1987-12-29 1989-07-14 Nitto Denko Corp Pressure-sensitive adhesive
JPH01178568A (en) 1987-12-29 1989-07-14 Nitto Denko Corp Pressure-sensitive adhesive
JPH10279900A (en) 1997-04-08 1998-10-20 Lintec Corp Self-adhesive sheet

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH05105857A (en) * 1991-08-21 1993-04-27 Sekisui Chem Co Ltd Self-adhesive composition and self-adhesive tape, label, or sheet
JPH073221A (en) * 1993-06-18 1995-01-06 Sekisui Chem Co Ltd Adhesive sheet for decoration
JP3498158B2 (en) * 1994-06-01 2004-02-16 綜研化学株式会社 Pressure sensitive adhesive composition for liquid crystal device and liquid crystal device
JPH1046126A (en) * 1996-08-01 1998-02-17 Nippon Synthetic Chem Ind Co Ltd:The Pressure-sensitive adhesive composition
JPH1046125A (en) * 1996-08-01 1998-02-17 Nippon Synthetic Chem Ind Co Ltd:The Pressure-sensitive adhesive composition
JP4383531B2 (en) * 1998-01-16 2009-12-16 日東電工株式会社 Pressure-sensitive adhesive sheets and methods for producing the same
KR100385720B1 (en) * 1999-04-30 2003-05-27 주식회사 엘지화학 Acrylic pressure-sensitive adhesive composition for optical use having improved rework property and laminates coated therewith
KR100383092B1 (en) * 1999-08-31 2003-05-12 주식회사 엘지화학 Acrylic pressure sensitive adhesives composition having superior residual stress relaxation effect

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01178567A (en) 1987-12-29 1989-07-14 Nitto Denko Corp Pressure-sensitive adhesive
JPH01178568A (en) 1987-12-29 1989-07-14 Nitto Denko Corp Pressure-sensitive adhesive
JPH10279900A (en) 1997-04-08 1998-10-20 Lintec Corp Self-adhesive sheet

Cited By (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6599967B2 (en) 2000-08-01 2003-07-29 Nitto Denko Corporation Pressure-sensitive adhesive sheet and method of fixing functional film
US20050014879A1 (en) * 2003-02-10 2005-01-20 Yutaka Moroishi Pressure sensitive adhesive composition for optical members, pressure sensitive adhesive layer for optical members, pressure sensitive adhesive optical member and image display
US7385007B2 (en) * 2003-02-12 2008-06-10 Nitto Denko Corporation Pressure sensitive adhesive composition for optical members, pressure sensitive adhesive layer for optical members, pressure sensitive adhesive optical member and image display
US20080213585A1 (en) * 2003-02-12 2008-09-04 Yutaka Moroishi Pressure sensitive adhesive composition for optical members, pressure sensitive adhesive layer for optical members, pressure sensitive adhesive optical member and image display
US7939604B2 (en) * 2003-02-12 2011-05-10 Nitto Denko Corporation Pressure sensitive adhesive composition for optical members, pressure sensitive adhesive layer for optical members, pressure sensitive adhesive optical member and image display
KR100988185B1 (en) * 2003-02-12 2010-10-18 닛토덴코 가부시키가이샤 Pressure sensitive adhesive composition for optical members, pressure sensitive adhesive layer for optical members, pressure sensitive adhesive optical member and image display
CN1683464B (en) * 2004-04-15 2010-05-05 日东电工株式会社 Adhesive composition for optical member, adhesive layer for optical member and its producing method, optical member with adhesive, and image display device
US20090022988A1 (en) * 2004-12-02 2009-01-22 Yuusuke Toyama Pressure sensitive adhesives for optical film, manufacturing methods for pressure sensitive adhesive layer for optical film, pressure sensitive adhesive layers for optical film, pressure sensitive adhesion type optical films and image displays
US7923120B2 (en) 2004-12-02 2011-04-12 Nitto Denko Corporation Adhesive of (meth)acrylate polymer, peroxide and isocyanate laminated on optical film
US8389611B2 (en) 2005-01-25 2013-03-05 Nitto Denko Corporation Pressure sensitive adhesive composition for optical members, pressure sensitive adhesive layer for optical members, pressure sensitive adhesive optical member and image display
US20090023869A1 (en) * 2005-01-25 2009-01-22 Nitto Denko Corporation Pressure sensitive adhesive composition for optical members, pressure sensitive adhesive layer for optical members, pressure sensitive adhesive optical member and image display
CN101107547B (en) * 2005-01-25 2011-06-22 日东电工株式会社 Pressure-sensitive adhesive composition for optical member, pressure-sensitive adhesive layer for optical member, pressure-sensitive adhesion type optical member, and image display device
US8088864B2 (en) * 2007-05-08 2012-01-03 Nitto Denko Corporation Pressure-sensitive adhesive composition, and pressure-sensitive adhesive product and display using the same
US20080281047A1 (en) * 2007-05-08 2008-11-13 Nitto Denko Corporation Pressure-sensitive adhesive composition, and pressure-sensitive adhesive product and display using the same
US20090104450A1 (en) * 2007-10-22 2009-04-23 Nitto Denko Corporation Pressure-sensitive adhesive composition for optical film, pressure-sensitive adhesive layer for optical film, production method thereof, pressure-sensitive adhesive optical film and image display
US8962135B2 (en) 2007-10-22 2015-02-24 Nitto Denko Corporation Pressure-sensitive adhesive composition for optical film, pressure-sensitive adhesive layer for optical film, production method thereof, pressure-sensitive adhesive optical film and image display
US20090162577A1 (en) * 2007-12-20 2009-06-25 Nitto Denko Corporation Pressure-sensitive adhesive composition for optical films, pressure-sensitive adhesive optical film and image display
US20100304134A1 (en) * 2008-01-25 2010-12-02 NITTO DENKO CORPORATION a corporation Method for peeling pressure-sensitive adhesive optical film, and pressure-sensitive adhesive optical film
US8685204B2 (en) * 2008-01-25 2014-04-01 Nitto Denko Corporation Method for peeling pressure-sensitive adhesive optical film, and pressure-sensitive adhesive optical film
US20100255253A1 (en) * 2009-04-01 2010-10-07 Nitto Denko Corporation Double-sided pressure-sensitive adhesive sheet, production method of double-sided pressure-sensitive adhesive sheet, pressure-sensitive adhesion type optical functional film and pressure-sensitive adhesion type hard coat film
CN101955738A (en) * 2009-07-16 2011-01-26 日东电工株式会社 Double-sided pressure-sensitive adhesive tape
US20110014410A1 (en) * 2009-07-16 2011-01-20 Nitto Denko Corporation Double-sided pressure-sensitive adhesive tape
CN101955738B (en) * 2009-07-16 2015-06-03 日东电工株式会社 Double-sided pressure-sensitive adhesive tape
US20110135810A1 (en) * 2009-12-03 2011-06-09 Marina Yakovleva Finely deposited lithium metal powder
US20120189835A1 (en) * 2011-01-25 2012-07-26 Nitto Denko Corporation Optical pressure-sensitive adhesive sheet
US20130123450A1 (en) * 2011-11-10 2013-05-16 Nitto Denko Corporation Pressure-sensitive adhesive sheet
US20150293287A1 (en) * 2012-08-31 2015-10-15 Nitto Denko Corporation Pressure-sensitive adhesive layer attached polarizing film and image display
US10422935B2 (en) * 2012-08-31 2019-09-24 Nitto Denko Corporation Pressure-sensitive adhesive layer attached polarizing film and image display

Also Published As

Publication number Publication date
KR100723113B1 (en) 2007-05-30
KR20010085543A (en) 2001-09-07
TWI241331B (en) 2005-10-11
JP2001234135A (en) 2001-08-28
JP3819661B2 (en) 2006-09-13
US20010021452A1 (en) 2001-09-13

Similar Documents

Publication Publication Date Title
US6451156B2 (en) Pressure-sensitive adhesive sheets and method of fixing functional film
US6599967B2 (en) Pressure-sensitive adhesive sheet and method of fixing functional film
EP1776433B1 (en) Acrylic pressure sensitive adhesive
EP1802724B1 (en) Acrylic pressure sensitive adhesive with good antistatic property
EP1781748B1 (en) Acrylic pressure sensitive adhesive having antistatic property
US8664326B2 (en) Acrylic pressure-sensitive adhesive composition
EP2044162B1 (en) Optically compensated acrylic pressure-sensitive adhesive composition, polarizing plate and liquid crystal display device containing the same
JP4776272B2 (en) Polymer composition for pressure-sensitive adhesive, pressure-sensitive adhesive composition for surface protective film, and surface protective film
EP2087060B1 (en) Acrylic pressure-sensitive adhesive composition for polarizing plate, containing a photo-initiator group
EP2226371A2 (en) Adhesive composition, and an adhesive polarising plate and liquid crystal display device comprising the same
EP1789512A1 (en) Acrylic pressure sensitive adhesive compositions
US8513363B2 (en) Adhesive composition
TWI753857B (en) Adhesive layer and adhesive film
KR100678795B1 (en) Pressure-sensitive adhesive compositions and adhesive films
KR100383092B1 (en) Acrylic pressure sensitive adhesives composition having superior residual stress relaxation effect
JPH09145925A (en) Self-adhesive polarizing plate
KR100405309B1 (en) Acrylic pressure sensitive adhesive for the polarizing firm
KR101541579B1 (en) Pressure-sensitive adhesive composition for an optical film
JPH08271883A (en) Glass cell laminated body for liquid crystal display
KR101770448B1 (en) Pressure sensitive adhesive composition
KR20200066216A (en) Coating composition
JP2020063428A (en) Light diffusion adhesive film

Legal Events

Date Code Title Description
AS Assignment

Owner name: NITTO DENKO CORPORATION, JAPAN

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:KISHIOKA, HIROAKI;OHURA, MASAHIRO;YOSHIKAWA, TAKAO;REEL/FRAME:011567/0134

Effective date: 20010208

FEPP Fee payment procedure

Free format text: PAYOR NUMBER ASSIGNED (ORIGINAL EVENT CODE: ASPN); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY

STCF Information on status: patent grant

Free format text: PATENTED CASE

FPAY Fee payment

Year of fee payment: 4

FPAY Fee payment

Year of fee payment: 8

FPAY Fee payment

Year of fee payment: 12